EP1420030A3 - Verfahren zur Synthese von (2S,3aS,7aS)-1-(S)-Alanyl-octahydro-1H-2-carbonsäurederivaten und Verwendung in der Synthese von Perindopril - Google Patents

Verfahren zur Synthese von (2S,3aS,7aS)-1-(S)-Alanyl-octahydro-1H-2-carbonsäurederivaten und Verwendung in der Synthese von Perindopril Download PDF

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Publication number
EP1420030A3
EP1420030A3 EP03293085A EP03293085A EP1420030A3 EP 1420030 A3 EP1420030 A3 EP 1420030A3 EP 03293085 A EP03293085 A EP 03293085A EP 03293085 A EP03293085 A EP 03293085A EP 1420030 A3 EP1420030 A3 EP 1420030A3
Authority
EP
European Patent Office
Prior art keywords
synthesis
perindopril
alanyl
octahydro
indole
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP03293085A
Other languages
English (en)
French (fr)
Other versions
EP1420030A2 (de
Inventor
Thierry Dubuffet
Jean-Pierre Lecouve
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Laboratoires Servier SAS
Original Assignee
Laboratoires Servier SAS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Laboratoires Servier SAS filed Critical Laboratoires Servier SAS
Priority to EP03293085A priority Critical patent/EP1420030A3/de
Publication of EP1420030A2 publication Critical patent/EP1420030A2/de
Publication of EP1420030A3 publication Critical patent/EP1420030A3/de
Priority to UAA200607607A priority patent/UA84897C2/uk
Priority to US10/582,419 priority patent/US7288661B2/en
Priority to JP2006543584A priority patent/JP2007537996A/ja
Priority to MYPI20045096A priority patent/MY136937A/en
Priority to PCT/FR2004/003167 priority patent/WO2005066199A1/fr
Priority to EA200601088A priority patent/EA010318B1/ru
Priority to CNB200480036942XA priority patent/CN100469787C/zh
Priority to PL380411A priority patent/PL380411A1/pl
Priority to AU2004312186A priority patent/AU2004312186A1/en
Priority to CA002548406A priority patent/CA2548406A1/fr
Priority to KR1020067013587A priority patent/KR20060096521A/ko
Priority to GEAP20049502A priority patent/GEP20084408B/en
Priority to NZ547555A priority patent/NZ547555A/en
Priority to BRPI0417540-9A priority patent/BRPI0417540A/pt
Priority to ZA200604368A priority patent/ZA200604368B/en
Priority to ARP040104614A priority patent/AR047328A1/es
Priority to MA29084A priority patent/MA28223A1/fr
Priority to NO20063027A priority patent/NO20063027L/no
Priority to HK07102977.6A priority patent/HK1095840A1/xx
Withdrawn legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06008Dipeptides with the first amino acid being neutral
    • C07K5/06017Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/06026Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atom, i.e. Gly or Ala
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Public Health (AREA)
  • Cardiology (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Peptides Or Proteins (AREA)
  • Indole Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
EP03293085A 2003-12-10 2003-12-10 Verfahren zur Synthese von (2S,3aS,7aS)-1-(S)-Alanyl-octahydro-1H-2-carbonsäurederivaten und Verwendung in der Synthese von Perindopril Withdrawn EP1420030A3 (de)

Priority Applications (20)

Application Number Priority Date Filing Date Title
EP03293085A EP1420030A3 (de) 2003-12-10 2003-12-10 Verfahren zur Synthese von (2S,3aS,7aS)-1-(S)-Alanyl-octahydro-1H-2-carbonsäurederivaten und Verwendung in der Synthese von Perindopril
UAA200607607A UA84897C2 (en) 2003-12-10 2004-09-12 Method for the synthesis of derivatives of (2s, 3as, 7as)-1-[(s)-alanyl]-octahydro-1h-indole-2-carboxylic acid and use thereof for the synthesis of perindopril
BRPI0417540-9A BRPI0417540A (pt) 2003-12-10 2004-12-09 processo de sìntese de derivados do ácido (2s, 3as, 7as)-1-[(s)-alanil]-octahidro-1h-indol-2-carboxìlico e aplicação para sìntese do perindopril
ZA200604368A ZA200604368B (en) 2003-12-10 2004-12-09 Method for the synthesis of derivatives of (2S, 3AS, 7AS)-1-[(S)-alanyl]-octahydro-1H-indole-2-carboxylic acid and use thereof for the synthesis of perindopril
AU2004312186A AU2004312186A1 (en) 2003-12-10 2004-12-09 Method for the synthesis of derivatives of (2S, 3aS, 7aS)-1-[(S)-alanyl]-octahydro-1H-indole-2-carboxylic acid and use thereof for the synthesis of perindopril
KR1020067013587A KR20060096521A (ko) 2003-12-10 2004-12-09 (2s,3as,7as)-1-[(s)-알라닐]-옥타히드로-1h-인돌-2-카르복실산 유도체의 합성 방법 및 페린도프릴의 합성을위한 상기 화합물의 용도
MYPI20045096A MY136937A (en) 2003-12-10 2004-12-09 NEW PROCESS FOR THE SYNTHESIS OF (2S, 3aS, 7aS)-1-[(S)-ALANYL]-OCTAHYDRO-1H-INDOLE-2-CARBOXYLIC ACID COMPOUNDS AND APPLICATION IN THE SYNTHESIS OF PERINDOPRIL
PCT/FR2004/003167 WO2005066199A1 (fr) 2003-12-10 2004-12-09 Procede de synthese de derives de l’acide (2s,3as,7as)-1-[(s)-alanyl]-octahydro-1h-indole-2-carboxylique et application a la synthese du perindopril
EA200601088A EA010318B1 (ru) 2003-12-10 2004-12-09 НОВЫЙ СПОСОБ СИНТЕЗА (2S,3aS,7aS)-1-[(S)-АЛАНИЛ]ОКТАГИДРО-1H-ИНДОЛ-2-КАРБОНОВЫХ КИСЛОТ И ИХ ПРИМЕНЕНИЕ В СИНТЕЗЕ ПЕРИНДОПРИЛА
CNB200480036942XA CN100469787C (zh) 2003-12-10 2004-12-09 合成(2s,3as,7as)-1-[(s)-1-丙氨酰基]-八氢-1h-吲哚-2-羧酸衍生物的方法及其用于合成培哚普利的用途
PL380411A PL380411A1 (pl) 2003-12-10 2004-12-09 Sposób otrzymywania pochodnych kwasu (2S, 3aS, 7aS)-1- [(S)-alanylo]oktahydro-1H-indolo-2- karboksylowego i zastosowanie ich do syntezy perindoprilu
US10/582,419 US7288661B2 (en) 2003-12-10 2004-12-09 Process for the synthesis of (2S,3aS,7aS)-1-[(S)-alanyl]-octahydro-1H-indole-2-carboxylic acid compounds and application in the synthesis of perindopril
CA002548406A CA2548406A1 (fr) 2003-12-10 2004-12-09 Nouveau procede de synthese de derives de l'acide (2s,3as,7as)-1-((s)-alanyl)-octahydro-1h-in-dole-2-carboxylique et application a la synthese du perindopril
JP2006543584A JP2007537996A (ja) 2003-12-10 2004-12-09 (2S,3aS,7aS)−1−[(S)−アラニル]オクタヒドロ−1H−インドール−2−カルボン酸の誘導体を合成する方法、およびペリンドプリルの合成のためのその使用
GEAP20049502A GEP20084408B (en) 2003-12-10 2004-12-09 Method for the synthesis of derivatives of (2s, 3as, 7as)-1-[(s)-alanyl]-octahydro-1h-indole-2-carboxylic acid and use thereof for the synthesis of perindopril
NZ547555A NZ547555A (en) 2003-12-10 2004-12-09 New process for the synthesis of (2S,3aS,7aS)-1-[(S)-alanyl]-octahydro-1H-indole-2-carboxylic acid compounds and application in the synthesis of perindopril
ARP040104614A AR047328A1 (es) 2003-12-10 2004-12-10 Procedimiento para la sintesis de compuestos del acido (2s, 3as, 7as)-1-[(s)-alanil]-octahidro-1h-indol-2-carboxilico y aplicacion en la sintesis de perindopril.
MA29084A MA28223A1 (fr) 2003-12-10 2006-06-07 NOUVEAU PROCEDE DE SYNTHESE DE DERIVES DE L'ACIDE (2S,3aS,7aS)-1-[(S)-ALANYL]-OCTAHYDRO-1H-INDOLE-2-CARBOXYLIQUE ET APPLICATION A LA SYNTHESE DU PERINDOPRIL
NO20063027A NO20063027L (no) 2003-12-10 2006-06-28 Fremgangsmaten for syntesen av derivater av (2S,3aS,7aS)-1-[(S)-alkanyl]-oktahydro-lH-indol-2-karboksylsyre og anvendelse derav i syntesen av perindopril
HK07102977.6A HK1095840A1 (en) 2003-12-10 2007-03-20 Method for the synthesis of derivatives of (2s,3as,7as)-1[(s)-alanyl]- octahydro-1h-indole-2-carboxylic acid and use thereof for the synthesis of perindopril

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP03293085A EP1420030A3 (de) 2003-12-10 2003-12-10 Verfahren zur Synthese von (2S,3aS,7aS)-1-(S)-Alanyl-octahydro-1H-2-carbonsäurederivaten und Verwendung in der Synthese von Perindopril

Publications (2)

Publication Number Publication Date
EP1420030A2 EP1420030A2 (de) 2004-05-19
EP1420030A3 true EP1420030A3 (de) 2004-05-26

Family

ID=32116382

Family Applications (1)

Application Number Title Priority Date Filing Date
EP03293085A Withdrawn EP1420030A3 (de) 2003-12-10 2003-12-10 Verfahren zur Synthese von (2S,3aS,7aS)-1-(S)-Alanyl-octahydro-1H-2-carbonsäurederivaten und Verwendung in der Synthese von Perindopril

Country Status (20)

Country Link
US (1) US7288661B2 (de)
EP (1) EP1420030A3 (de)
JP (1) JP2007537996A (de)
KR (1) KR20060096521A (de)
CN (1) CN100469787C (de)
AR (1) AR047328A1 (de)
AU (1) AU2004312186A1 (de)
BR (1) BRPI0417540A (de)
CA (1) CA2548406A1 (de)
EA (1) EA010318B1 (de)
GE (1) GEP20084408B (de)
HK (1) HK1095840A1 (de)
MA (1) MA28223A1 (de)
MY (1) MY136937A (de)
NO (1) NO20063027L (de)
NZ (1) NZ547555A (de)
PL (1) PL380411A1 (de)
UA (1) UA84897C2 (de)
WO (1) WO2005066199A1 (de)
ZA (1) ZA200604368B (de)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1256590A1 (de) * 2001-07-24 2002-11-13 Les Laboratoires Servier S.A. Verfahren zur Synthese von (2S,3aS,7aS)-1-(S)-Alanyl-octahydro-1H-2-carbonsäurederivaten und Verwendung in der Synthese von Perindopril

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2620709B1 (fr) * 1987-09-17 1990-09-07 Adir Procede de synthese industrielle du perindopril et de ses principaux intermediaires de synthese

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1256590A1 (de) * 2001-07-24 2002-11-13 Les Laboratoires Servier S.A. Verfahren zur Synthese von (2S,3aS,7aS)-1-(S)-Alanyl-octahydro-1H-2-carbonsäurederivaten und Verwendung in der Synthese von Perindopril

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
CARPINO, LOUIS A. ET AL: "Effect of Tertiary Bases on O-Benzotriazolyluronium Salt-Induced Peptide Segment Coupling", JOURNAL OF ORGANIC CHEMISTRY (1994), 59(4), 695-8, XP002273951 *
CHEN, SHAOQING ET AL: "A new coupling reagent for peptide synthesis. Benzotriazolyloxybis(pyrrolidino)carbonium hexafluorophosphate (BBC)", TETRAHEDRON LETTERS (1992), 33(5), 647-50, XP001180313 *
COSTE, JACQUES ET AL: "Oxybenzotriazole free peptide coupling reagents for N-methylate amino acids", TETRAHEDRON LETTERS (1991), 32(17), 1967-70, XP001180312 *
LI P ET AL: "THE DEVELOPMENT OF HIGHLY EFFICIENT ONIUM-TYPE PEPTIDE COUPLING REAGENTS BASED UPON RATIONAL MOLECULAR DESIGN", JOURNAL OF PEPTIDE RESEARCH, MUNKSGAARD INTERNATIONAL PUBLISHERS, COPENHAGEN, DK, vol. 58, no. 2, 1 August 2001 (2001-08-01), pages 129 - 139, XP001039108, ISSN: 1397-002X *
LI, PENG ET AL: "BOMI - a novel peptide coupling reagent", TETRAHEDRON LETTERS (1999), 40(18), 3605-3608, XP004162348 *
LI, PENG ET AL: "New and highly efficient immonium-type peptide coupling reagents: synthesis, mechanism, and application", TETRAHEDRON (2000), 56(26), 4437-4445, XP004202135 *

Also Published As

Publication number Publication date
MA28223A1 (fr) 2006-10-02
WO2005066199A1 (fr) 2005-07-21
CN100469787C (zh) 2009-03-18
CA2548406A1 (fr) 2005-07-21
UA84897C2 (en) 2008-12-10
JP2007537996A (ja) 2007-12-27
AR047328A1 (es) 2006-01-18
US7288661B2 (en) 2007-10-30
AU2004312186A1 (en) 2005-07-21
NZ547555A (en) 2009-11-27
MY136937A (en) 2008-11-28
US20070123581A1 (en) 2007-05-31
CN1890259A (zh) 2007-01-03
ZA200604368B (en) 2007-10-31
HK1095840A1 (en) 2007-05-18
NO20063027L (no) 2006-06-28
GEP20084408B (en) 2008-06-25
EP1420030A2 (de) 2004-05-19
KR20060096521A (ko) 2006-09-12
PL380411A1 (pl) 2007-01-22
EA200601088A1 (ru) 2006-12-29
EA010318B1 (ru) 2008-08-29
BRPI0417540A (pt) 2007-03-27

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